Evidence map›Paper›PMID 31428099›Full record

ArticleFrontiers in immunology2019

Anti-CXCR4 Antibody Combined With Activated and Expanded Natural Killer Cells for Sarcoma Immunotherapy.

Maria Vela, David Bueno, Pablo González-Navarro, Ariadna Brito, Lucía Fernández, Adela Escudero, Jaime Valentín, Carmen Mestre-Durán, Marina Arranz-Álvarez, Rebeca Pérez de Diego and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

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  10. CXCL12-CXCR4/CXCR7 Axis in Cancer: from Mechanisms to Clinical Applications.International journal of biological sciences · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 1 country.

Maria VelaTranslational Research in Pediatric Oncology, Hematopoietic Transplantation and Cell Therapy, Hospital La Paz Institute for Health Research (IdiPAZ), Madrid, Spain.
David BuenoPediatric Hemato-Oncology Department, Hospital Universitario La Paz, Madrid, Spain.
Pablo González-NavarroTranslational Research in Pediatric Oncology, Hematopoietic Transplantation and Cell Therapy, Hospital La Paz Institute for Health Research (IdiPAZ), Madrid, Spain.
Ariadna BritoTranslational Research in Pediatric Oncology, Hematopoietic Transplantation and Cell Therapy, Hospital La Paz Institute for Health Research (IdiPAZ), Madrid, Spain.
Lucía FernándezH12O-CNIO Hematological Malignancies Clinical Research Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Adela EscuderoMolecular Pediatric Oncology Unit, Institute of Medical and Molecular Genetics (INGEMM), La Paz University Hospital, Madrid, Spain.
Jaime ValentínTranslational Research in Pediatric Oncology, Hematopoietic Transplantation and Cell Therapy, Hospital La Paz Institute for Health Research (IdiPAZ), Madrid, Spain.
Carmen Mestre-DuránTranslational Research in Pediatric Oncology, Hematopoietic Transplantation and Cell Therapy, Hospital La Paz Institute for Health Research (IdiPAZ), Madrid, Spain.
Marina Arranz-ÁlvarezBiobank of Hospital La Paz Institute for Health Research (IdiPAZ), Madrid, Spain.
Rebeca Pérez de DiegoLaboratory of Immunogenetics of Human Diseases, Hospital La Paz Institute for Health Research (IdiPAZ), Madrid, Spain.
Marta MendiolaMolecular Pathology and Therapeutic Targets, Hospital La Paz Institute for Health Research (IdiPAZ), Madrid, Spain.
José Juan Pozo-KreilingerMolecular Pathology and Therapeutic Targets, Hospital La Paz Institute for Health Research (IdiPAZ), Madrid, Spain.
Antonio Pérez-MartínezPediatric Hemato-Oncology Department, Hospital Universitario La Paz, Madrid, Spain.
Hospital La Paz Institute for Health Research · ESHospital Universitario La Paz · ESCentro de Investigación en Red en Enfermedades Cardiovasculares · ESSpanish National Cancer Research Centre · ESUniversidad Autónoma de Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sarcoma is one of the most severe forms of pediatric cancer and current therapies -chemotherapy and surgery- fail to eradicate the disease in half of patients. Preclinical studies combining new therapeutic approaches can be useful to design better therapies. On one hand, it is known that CXCR4 expression is implicated in rhabdomyosarcoma progression, so we analyzed relapses and chemotherapy-resistant rhabdomyosarcoma tumors from pediatric patients and found that they had particularly high levels of CXCR4 expression. Moreover, in assays

Indexed as

AnimalsAntibodies, MonoclonalCell Line, TumorCytotoxicity, ImmunologicFemaleHumansImmunologic FactorsImmunotherapyImmunotherapy, AdoptiveKiller Cells, NaturalLung NeoplasmsMiceMice, Inbred NODReceptors, CXCR4RhabdomyosarcomaSarcomaAntibodies, MonoclonalCXCR4 protein, humanImmunologic FactorsReceptors, CXCR4activated and expanded natural killer (NKAE) cellschemokine C-X-C receptor 4 (CXCR4)immunotherapymetastasissarcomatherapeutic antibody

Identifiers

PMID31428099
PMCPMC6688426
OpenAlexW4229638581

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.